# Fci (France Chirurgie Instrumentation) Sas

- Location (FDA's records): Paris, FR
- FDA decisions: 8 (2012–2022): 8 510(k) clearances
- Names in FDA's records: Fci (France Chirurgie Instrumentation) Sas (4); Fci Sas (France Chirurgie Instrumentation) (3); Fci (France Chirurgie Instrumentation) (1)
- Product codes: OKS (6), HPZ (1), NCB (1)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 4 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Fci Ophthalmics, Inc.: 4 (https://510kreport.com/company/fci-ophthalmics)
- Porex Surgical, Inc.: 1 (https://510kreport.com/company/porex-surgical)
- Hiroyasu Higuchi: 1 (https://510kreport.com/company/hiroyasu-higuchi)
- Meddev Corp.: 1 (https://510kreport.com/company/meddev)
- G.W.B. Intl., Ltd.: 1 (https://510kreport.com/company/gwb-intl)
- Eagle Vision, Inc.: 1 (https://510kreport.com/company/eagle-vision)

## Firms that cite its devices most
- Anodyne: 1 (https://510kreport.com/company/anodyne)

## Its most-cited devices
- K121142: Crawford Biocanaliculus Intubation (2012), cited by 2
- K130375: Self-Retaining Bicanaliculus Intubaton Set II (2013), cited by 1
- K113536: Masterka 40 Masterka 35 Masterka 30 (2012), cited by 1

## Recent decisions
- K212741: Ezypor (Jun 24, 2022)
- K203569: Gold Tapered Weight Eyelid Implants, Platinum Tapered Weight Eyelid Implants (Jun 11, 2021)
- K201892: Ritleng®+ and Ritleng®+ PVP (Mar 11, 2021)
- K201606: LacriJet® (Dec 18, 2020)
- K161373: Nunchaku (Nov 3, 2016)
- K130375: Self-Retaining Bicanaliculus Intubaton Set II (Dec 4, 2013)
- K121142: Crawford Biocanaliculus Intubation (Aug 9, 2012)
- K113536: Masterka 40 Masterka 35 Masterka 30 (Aug 3, 2012)

Source page: https://510kreport.com/company/fci-france-chirurgie-instrumentation